A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364214



Internal ID21021767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177196101..177198200hg38UCSC Ensembl
chr3:176913889..176915988hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099684
Samples
Known GenesTBL1XR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364214
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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